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Cobalt-based ZIF coordinated hybrids with defective TiO for boosting visible light-driven photo-Fenton-like degradation of bisphenol A. | LitMetric

Cobalt-based ZIF coordinated hybrids with defective TiO for boosting visible light-driven photo-Fenton-like degradation of bisphenol A.

Chemosphere

School of Chemistry and Chemical Engineering, Tianjin University of Technology, Tianjin, 300384, PR China; Tianjin Key Laboratory of Organic Solar Cells and Photochemical Conversion, Tianjin, 300384, PR China. Electronic address:

Published: November 2020

Designing heterostructure of photocatalyst as an efficient approach to boost visible light-driven photocatalytic degradation, we prepared a series of cobalt-based ZIF coordinated with defective TiO, denoted as B-TiO@ZIF-67 composites, through wrapping defective B-TiO on ZIF-67 for promoting photocatalytic degradation efficiency of biphenyl A. The B-TiO@ZIF-67 composites displayed superior photocatalytic performance to pure TiO or ZIF-67 because of faster separation of photogenerated charge carriers and more suitable redox potentials. Such a novel photo-Fenton-like system composed of B-TiO@ZIF-67/HO/visible light accelerated the peroxidative degradation of biphenyl An up to a removal efficiency of 95.30%, which is also higher than that of photocatalysis or Fenton-like reaction alone. In addition, the degradation efficiency of biphenyl A is unchanged after catalyst reuse of four cycles. Integrating the trapping experiments and electrochemical analysis, we found the oxygen vacancy on B-TiO capturing the electrons to promote the separation of photogenerated charges, meanwhile the Co(II) in the composite decomposed hydrogen peroxide (HO) to produce more •OH radical. Both of them mutually boosted the removal efficiency. Finally, feasible degradation pathways of biphenyl A were proposed based on the assay of LC-MS spectrometry. This strategy offers a novel insight into fabrication of Co-ZIF-based TiO materials and application to visible light-driven photocatalytic and Fenton-like degradation reaction.

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Source
http://dx.doi.org/10.1016/j.chemosphere.2020.127431DOI Listing

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